The ability to unambiguously mark a cell's genotype is essential for studie
s in which genetically distinct cell populations must be distinguished from
one another in vivo. One approach to this challenge has been the creation
of transgenic mice expressing a transgene marker that is easily detectable,
with no background staining. Multiple transgenic mouse strains bearing con
structs with different combinations of promoter elements and coding sequenc
es have been described, each with its own advantages and limitations. In th
is report we describe the use of an 800-bp promoter fragment isolated from
the beta geo integration site in ROSA26 mice to target expression of two ma
rker genes. We demonstrate that the ROSA26 promoter directs ubiquitous expr
ession of human placental alkaline phosphatase and enhanced green fluoresce
nt protein during embryonic and postnatal development in mouse and rat. We
further demonstrate the general utility of these transgenes for marking don
or cells in transplantation studies. (C) 1999 Academic Press.